510(k) Report

FDA applicant

Seattle Artificial Kidney Supply Co.

Mchenry, IL1 decision1976–19760 recalls

FDA records 1 decision for Seattle Artificial Kidney Supply Co. (Mchenry, IL) in 1976: 1 510(k) clearance. All are in product code FKQ (System, Dialysate Delivery, Central Multiple…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Seattle Artificial Kidney Supply Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Seattle Artificial Kidney Supply Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Seattle Artificial Kidney Supply Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Seattle”

FDA records each applicant name separately; these may or may not be the same firm.